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The ESRP1-GPR137 axis contributes to intestinal pathogenesis
Aberrant alternative pre-mRNA splicing (AS) events have been associated with several disorders. However, it is unclear whether deregulated AS directly contributes to disease. Here, we reveal a critical role of the AS regulator epithelial splicing regulator protein 1 (ESRP1) for intestinal homeostasi...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665647/ https://www.ncbi.nlm.nih.gov/pubmed/28975893 http://dx.doi.org/10.7554/eLife.28366 |
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author | Mager, Lukas Franz Koelzer, Viktor Hendrik Stuber, Regula Thoo, Lester Keller, Irene Koeck, Ivonne Langenegger, Maya Simillion, Cedric Pfister, Simona P Faderl, Martin Genitsch, Vera Tcymbarevich, Irina Juillerat, Pascal Li, Xiaohong Xia, Yu Karamitopoulou, Eva Lyck, Ruth Zlobec, Inti Hapfelmeier, Siegfried Bruggmann, Rémy McCoy, Kathy D Macpherson, Andrew J Müller, Christoph Beutler, Bruce Krebs, Philippe |
author_facet | Mager, Lukas Franz Koelzer, Viktor Hendrik Stuber, Regula Thoo, Lester Keller, Irene Koeck, Ivonne Langenegger, Maya Simillion, Cedric Pfister, Simona P Faderl, Martin Genitsch, Vera Tcymbarevich, Irina Juillerat, Pascal Li, Xiaohong Xia, Yu Karamitopoulou, Eva Lyck, Ruth Zlobec, Inti Hapfelmeier, Siegfried Bruggmann, Rémy McCoy, Kathy D Macpherson, Andrew J Müller, Christoph Beutler, Bruce Krebs, Philippe |
author_sort | Mager, Lukas Franz |
collection | PubMed |
description | Aberrant alternative pre-mRNA splicing (AS) events have been associated with several disorders. However, it is unclear whether deregulated AS directly contributes to disease. Here, we reveal a critical role of the AS regulator epithelial splicing regulator protein 1 (ESRP1) for intestinal homeostasis and pathogenesis. In mice, reduced ESRP1 function leads to impaired intestinal barrier integrity, increased susceptibility to colitis and altered colorectal cancer (CRC) development. Mechanistically, these defects are produced in part by modified expression of ESRP1-specific Gpr137 isoforms differently activating the Wnt pathway. In humans, ESRP1 is downregulated in inflamed biopsies from inflammatory bowel disease patients. ESRP1 loss is an adverse prognostic factor in CRC. Furthermore, generation of ESRP1-dependent GPR137 isoforms is altered in CRC and expression of a specific GPR137 isoform predicts CRC patient survival. These findings indicate a central role of ESRP1-regulated AS for intestinal barrier integrity. Alterations in ESRP1 function or expression contribute to intestinal pathology. |
format | Online Article Text |
id | pubmed-5665647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56656472017-11-03 The ESRP1-GPR137 axis contributes to intestinal pathogenesis Mager, Lukas Franz Koelzer, Viktor Hendrik Stuber, Regula Thoo, Lester Keller, Irene Koeck, Ivonne Langenegger, Maya Simillion, Cedric Pfister, Simona P Faderl, Martin Genitsch, Vera Tcymbarevich, Irina Juillerat, Pascal Li, Xiaohong Xia, Yu Karamitopoulou, Eva Lyck, Ruth Zlobec, Inti Hapfelmeier, Siegfried Bruggmann, Rémy McCoy, Kathy D Macpherson, Andrew J Müller, Christoph Beutler, Bruce Krebs, Philippe eLife Cancer Biology Aberrant alternative pre-mRNA splicing (AS) events have been associated with several disorders. However, it is unclear whether deregulated AS directly contributes to disease. Here, we reveal a critical role of the AS regulator epithelial splicing regulator protein 1 (ESRP1) for intestinal homeostasis and pathogenesis. In mice, reduced ESRP1 function leads to impaired intestinal barrier integrity, increased susceptibility to colitis and altered colorectal cancer (CRC) development. Mechanistically, these defects are produced in part by modified expression of ESRP1-specific Gpr137 isoforms differently activating the Wnt pathway. In humans, ESRP1 is downregulated in inflamed biopsies from inflammatory bowel disease patients. ESRP1 loss is an adverse prognostic factor in CRC. Furthermore, generation of ESRP1-dependent GPR137 isoforms is altered in CRC and expression of a specific GPR137 isoform predicts CRC patient survival. These findings indicate a central role of ESRP1-regulated AS for intestinal barrier integrity. Alterations in ESRP1 function or expression contribute to intestinal pathology. eLife Sciences Publications, Ltd 2017-10-04 /pmc/articles/PMC5665647/ /pubmed/28975893 http://dx.doi.org/10.7554/eLife.28366 Text en © 2017, Mager et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cancer Biology Mager, Lukas Franz Koelzer, Viktor Hendrik Stuber, Regula Thoo, Lester Keller, Irene Koeck, Ivonne Langenegger, Maya Simillion, Cedric Pfister, Simona P Faderl, Martin Genitsch, Vera Tcymbarevich, Irina Juillerat, Pascal Li, Xiaohong Xia, Yu Karamitopoulou, Eva Lyck, Ruth Zlobec, Inti Hapfelmeier, Siegfried Bruggmann, Rémy McCoy, Kathy D Macpherson, Andrew J Müller, Christoph Beutler, Bruce Krebs, Philippe The ESRP1-GPR137 axis contributes to intestinal pathogenesis |
title | The ESRP1-GPR137 axis contributes to intestinal pathogenesis |
title_full | The ESRP1-GPR137 axis contributes to intestinal pathogenesis |
title_fullStr | The ESRP1-GPR137 axis contributes to intestinal pathogenesis |
title_full_unstemmed | The ESRP1-GPR137 axis contributes to intestinal pathogenesis |
title_short | The ESRP1-GPR137 axis contributes to intestinal pathogenesis |
title_sort | esrp1-gpr137 axis contributes to intestinal pathogenesis |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5665647/ https://www.ncbi.nlm.nih.gov/pubmed/28975893 http://dx.doi.org/10.7554/eLife.28366 |
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